ER-lysosome lipid transfer protein VPS13C/PARK23 prevents aberrant mtDNA-dependent STING signaling

Mutations in VPS13C cause early-onset, autosomal recessive Parkinson’s disease (PD). We have established that VPS13C encodes a lipid transfer protein localized to contact sites between the ER and late endosomes/lysosomes. In the current study, we demonstrate that depleting VPS13C in HeLa cells causes an accumulation of lysosomes with an altered lipid profile, including an accumulation of di-22:6-BMP, a biomarker of the PD-associated leucine-rich repeat kinase 2 (LRRK2) G2019S mutation. In addition, the DNA-sensing cGAS-STING pathway, which was recently implicated in PD pathogenesis, is activated in these cells. This activation results from a combination of elevated mitochondrial DNA in the cytosol and a defect in the degradation of activated STING, a lysosome-dependent process. These results suggest a link between ER-lysosome lipid transfer and innate immune activation in a model human cell line and place VPS13C in pathways relevant to PD pathogenesis.     

LRG‐1 promotes fat graft survival through the RAB31‐mediated inhibition of hypoxia‐induced apoptosis

Autologous adipose tissue is an ideal soft tissue filling material, and its biocompatibility is better than that of artificial tissue substitutes, foreign bodies and heterogeneous materials. Although autologous fat transplantation has many advantages, the low retention rate of adipose tissue limits its clinical application. Here, we identified a secretory glycoprotein, leucine‐rich‐alpha‐2‐glycoprotein 1 (LRG‐1), that could promote fat graft survival through RAB31‐mediated inhibition of hypoxia‐induced apoptosis. We showed that LRG‐1 injection significantly increased the maintenance of fat volume and weight compared with the control. In addition, higher fat integrity, more viable adipocytes and fewer apoptotic cells were observed in the LRG‐1‐treated groups. Furthermore, we discovered that LRG‐1 could reduce the ADSC apoptosis induced by hypoxic conditions. The mechanism underlying the LRG‐1‐mediated suppression of the ADSC apoptosis induced by hypoxia was mediated by the upregulation of RAB31 expression. Using LRG‐1 for fat grafts may prove to be clinically successful for increasing the retention rate of transplanted fat.     

鄱阳湖浮游甲壳动物群落结构特征

鄱阳湖是中国第一大淡水湖,具有"丰水为湖,枯水为河"的独特特点。为探讨鄱阳湖浮游甲壳动物群落结构及其时空分布的特征,于2009年全年采集其不同季节、不同水位期的浮游甲壳动物样品进行定量分析。结果显示,鄱阳湖浮游甲壳动物群落结构总体与河流浮游甲壳群落具有相似性。无节幼体、象鼻溞、剑水蚤等河流优势类群在鄱阳湖浮游甲壳动物中占优势;而哲水蚤和溞属仅在低水位季节占优势,枝角类丰度仅在高温、高水位、流速缓的季节高过桡足类。丰水期浮游甲壳动物平均丰度和生物量远远高于枯水期,可达枯水期的50倍,差异极其显著(P0.01)。温度和水位变化引起的环境因子改变是导致鄱阳湖浮游甲壳动物发生季节演替的主要原因;而营养盐对浮游甲壳动物的影响并不显著。空间上浮游甲壳动物群落构成明显不同,年均丰度最高和最低的点均出现在河口地区。因此:对于换水周期短,水交换速率快的水体,应该充分考虑水文条件对生物的影响。     

Rhabdomyolysis happened after the start of dabigatran etexilate treatment: A case report

There are few reports of rhabdomyolysis caused by anticoagulants, and it is extremely rare for it to be caused by dabigatran etexilate. An 86-year-old female experienced sudden muscle weakness and pain, a significant increase in Creatine kinase, and renal impairment after oral administration of dabigatran etexilate for 3 weeks. The enhanced thigh MRI showed abnormal signal in multiple thigh muscle groups, indicating that the lesions should be considered inflammatory diseases. In conclusion, the possibility of rhabdomyolysis should be ruled out when muscle weakness and myalgia occur at the beginning of dabigatran etexilate treatment.     

黑河流域叶面积指数（LAI）空间尺度转换

为有机地整合利用不同分辨率遥感数据获取的陆面过程以及其他相关的环境变量,尺度问题越来越受到人们的重视.选取黑河张掖绿洲区为实验研究区,利用ETM 影像反演的LAI通过升尺度转换到900m分辨率,对LAI尺度转换过程中引起的误差进行了定量分析,尝试提出一种新的基于NDVI像元分解的更有效的升尺度转换方法.研究发现非线性的升尺度算法引起的误差不超过 10.5%,且误差大小与地表异质性程度正相关,而地表异质性是导致LAI尺度转化误差的主要原因,严重时可能造成 45%的偏差,但纯像元LAI的计算不受尺度影响.提出的基于NDVI像元分解的LAI升尺度转换算法,分两步考虑了地表异质性问题,很好的实现了研究区30m空间精度 LAI向900m的尺度转换,该方法应用于干旱、半干旱的中国西北黑河流域NASA 发布的MODIS LAI产品校正,取得了良好效果.     

中国增汇型气候保护政策实施对经济的影响

系统地给出了中国实施增汇型CO2减排政策对宏观经济影响的模拟结果,所采用的模拟系统包括基于Pizer,Demeter,Zwaan工作发展的中国气候保护决策支持系统和中国经济可计算一般均衡(CGE)系统。研究结果表明,增汇型气候保护政策较其他单一的气候保护政策更有利于国家经济安全;虽然增汇型气候保护政策在短期内会对国家GDP产出造成影响,但从长远角度看,增汇型气候保护将带动经济的发展,是一项值得推广的减排政策。同时,发现中国实行每年增加4%的碳汇和实施4%能源替代以减少CO2排放控制率,辅助于0.2%的生产型CO2排放控制率,如果能够促进世界其它地区到2050年减排1990年的10%的CO,是一个合适的方案。     

胶茶群落及胶林、茶园太阳辐射光谱的研究

1983—1985年,我们进行了胶茶人工群落及胶林、茶园对太阳辐射光谱吸收利用状况的探索研究。着重对可见光谱区的两个吸收带,4000—5000(?)(蓝紫光)、6000—7600A(红橙光)以及红外光谱区的10000—13200(?)(近红外)、14800—18000(?)(远红外)进行了分析讨论,以期从生态和生理的角度阐明群落结构比单一结构的优越性及其对胶、茶产量和品质的影响。     

上皮细胞K+通道的生理学意义与临床应用:跨上皮细胞转运的驱动力生成和K+循环

K^＋通道在上皮细胞内以极化的方式表达,形成一个庞大的膜蛋白家族。出于对主要依赖Na^＋-K^＋-ATPase而维持的细胞内跨膜K^＋梯度的考虑,K^＋通道在跨上皮细胞转运中的主要作用为：膜电位生成和K^＋循环。本文以肾近端小管和胃壁上皮细胞转运为例简要阐述了K^＋通道的作用。在这两个组织中,K^＋通道活性限速跨上皮细胞转运,调节细胞体积。近年来,药理学工具和转基因动物的实验证实了对K^＋通道的原先认知,并将研究深入到分子水平。K^＋通道的分子结构挑战高亲和力药物分子的设计,及其多组织同时表达的两个典型特征阻碍了高活性、组织特异性小分子治疗的进展。然而,抑制K^＋通道能阻断胃酸分泌等病理生理机制的深入研究,促进K^＋通道药物用于胃病治疗和作为肾脏转运抑制剂用于肾脏相关疾病治疗。